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Journal of Clinical Medicine logoLink to Journal of Clinical Medicine
. 2018 Dec 15;7(12):553. doi: 10.3390/jcm7120553

Health-Related Quality of Life in Chronic Liver Diseases: A Strong Impact of Hand Grip Strength

Hiroki Nishikawa 1, Hirayuki Enomoto 1,*, Kazunori Yoh 1, Yoshinori Iwata 1, Yoshiyuki Sakai 1, Kyohei Kishino 1, Naoto Ikeda 1, Tomoyuki Takashima 1, Nobuhiro Aizawa 1, Ryo Takata 1, Kunihiro Hasegawa 1, Noriko Ishii 1, Yukihisa Yuri 1, Takashi Nishimura 1, Hiroko Iijima 1, Shuhei Nishiguchi 1
PMCID: PMC6306870  PMID: 30558298

Abstract

We sought to examine the influence of hand grip strength (HGS) and skeletal muscle mass (SMM) on the health-related quality of life (H-QOL) as evaluated by the 36-Item Short-Form Health Survey (SF-36) questionnaire in chronic liver diseases (CLDs, 198 men and 191 women). Decreased HGS was defined as HGS <26 kg for men and <18 kg for women. Decreased SMM was defined as SMM index <7.0 kg/m2 for men and <5.7 kg/m2 for women, using bioimpedance analysis. SF-36 scores were compared between groups stratified by HGS or SMM. Between-group differences (decreased HGS vs. non-decreased HGS) in the items of physical functioning (PF), role physical (RP), bodily pain, vitality (VT), social functioning (SF), role emotional (RE), and physical component summary score (PCS) reached significance, while between-group differences (decreased SMM vs. non-decreased SMM) in the items of PF, SF and RE were significant. Multivariate analyses revealed that HGS was significantly linked to PF (p = 0.0031), RP (p = 0.0185), and PCS (p = 0.0421) in males, and PF (p = 0.0034), VT (p = 0.0150), RE (p = 0.0422), and PCS (p = 0.0191) in females. HGS had a strong influence especially in the physiological domains in SF-36 in CLDs.

Keywords: Chronic liver disease, Health-related quality of life, SF-36, Hand grip strength, Skeletal muscle mass

1. Introduction

The health-related quality of life (H-QOL) is a patient-centered clinical outcome that is used internationally for patients with various diseases, including diabetes mellitus, and cardiovascular diseases, renal diseases and malignancies [1,2,3,4]. Chronic liver diseases (CLDs) can also affect H-QOL [5,6,7,8,9]. Due to the adverse clinical and patient-reported outcomes, and the economic burden of CLDs, improving H-QOL in patients with CLDs should be a major treatment goal [5,6,7,8,9]. A previous study reported that higher H-QOL was associated with favorable clinical outcome in patients with CLDs and increasing the number of pivotal clinical trials have adopted H-QOL as additional study endpoints [10,11]. The most extensively used assessment methods for H-QOL is the 36-Item Short Form Health Survey (SF-36) [12,13,14,15,16].

Skeletal muscle mass (SMM) increases till 20 years, peaks between 20 and 50 years, and decreases by approximately 1% after the age of 50 years, due to changes in muscle fiber type and size [17]. Sarcopenia is a clinical disease entity that is defined by diminished muscle function and SMM [18,19,20,21,22,23,24,25,26,27,28]. It can be associated with worse clinical outcomes and higher health care costs in various diseases, and there is therefore urgent need for the establishment of methods for improving sarcopenia [18,19,20,21,22,23,24,25,26,27,28]. This also applies to CLD patients [19,21,23]. Sarcopenia is the main component of malnutrition, and it is primarily responsible for the unfavorable clinical consequences that are observed in CLD patients [19,21,23]. Liver cirrhosis (LC) can easily complicate sarcopenia, due to impaired protein synthesis [19]. Currently, the Japanese Society of Hepatology (JSH) reported that the original criteria for sarcopenia in liver diseases, with reference to the Asian criteria for sarcopenia [18,22]. The JSH criteria use hand grip strength (HGS) for muscle strength assessment, and bioimpedance analysis (BIA) and/or computed tomography for muscle mass assessment, while unlike the Asian criteria for sarcopenia, there is no age restriction for the assessment of sarcopenia in the JSH criteria, because younger patients with severe advanced CLDs such as liver failure are likely to be involved in sarcopenia [18].

However, as far as we are aware, scarce data regarding the relevance between H-QOL and HGS and SMM in CLD patients are currently available, although there are several reports where it is not diminished SMM, but diminished muscle strength, that is related to the weakness of physical function in patients with diabetes-related dementia, and that HGS is an important correlate of health in breast cancer survivors [29,30]. We hypothesized that HGS rather than SMM may affect H-QOL in CLD patients. To clarify these clinical research questions, we primarily sought to examine the influence of HGS and SMM on H-QOL, as evaluated by the SF-36 questionnaire, as compared with other clinical data (liver functional data, nutritional data, etc.) in patients with CLDs.

2. Patients and Methods

2.1. Patients

A total of 410 CLD patients with data for HGS and SMM, using BIA and the SF-36 scores available were admitted to our hospital between November 2013 and August 2018. Each attending physician asked study subjects to receive body composition analysis, and to complete SF-36 questionnaires. Of these, 15 patients with hepatic encephalopathy, advanced malignancies, severe inflammatory diseases, or severe psychiatric diseases that potentially affect H-QOL were excluded. Six subjects with severe ascites were also excluded from the study subjects, because BIA can be challenging in patients with severe fluid retention, that is, overestimates could occur in the calculation of skeletal muscle mass index (SMI) by using BIA in such patients [19]. Three hundred and eighty-nine patients were therefore analyzed. LC was determined using histological and/or imaging studies. FIB-4 index as determined by age, aspartate aminotransferase, alanine aminotransferase, and platelet count, and the controlling nutritional (CONUT) score as determined by serum albumin value, total cholesterol value, and lymphocyte count, were calculated as described elsewhere [31,32].

2.2. Questionnaire

Study subjects were asked to complete the Japanese version of the SF-36 (self-reported questionnaire). It consists of 36 items and is classified into multi-item (eight items) scales: physical functioning (PF), role physical (RP), bodily pain (BP), general health perception (GH), vitality (VT), social functioning (SF), role emotion (RE), and mental health (MH) [33]. The physical component summary score (PCS) and the mental component summary score (MCS) were additionally included in this questionnaire, and its validity was well confirmed [33]. Thus, a total of 10 items were evaluated.

2.3. Measurement of HGS and SMI

The measurement of HGS was based on the current guidelines [18]. Two measurements of HGS were performed on both the left and right sides. The better measurement on each side was used, and HGS was calculated as the mean of these values. SMI was defined as “appendicular SMM/(height (m))2” using BIA. Based on the current guidelines, patients with decreased HGS (d-HGS) were defined as those with HGS < 26 kg for men and <18 kg for women. Similarly, patients with decreased SMM (d-SMM) were defined as those with SMI < 7.0 kg/m2 for men and <5.7 kg/m2 for women [18]. As described earlier, the JSH criteria for sarcopenia in liver disease determines sarcopenia based on muscle strength and muscle mass regardless of age, because younger patients with advanced LC status may be involved in sarcopenia [18].

First, the impacts of HGS and SMM on the SF-36 scores across 10 items were examined for all cases and several subgroups according to the LC status, gender, and age. Subsequently, the relationships between the SF-36 scores across 10 items and baseline data were investigated. Factors associated with the SF-36 scores were also studied by using multivariate analysis. We received the ethical approval from the ethics committee of our hospital (approval no, 2296). The protocol in the study strictly observed all regulations of the Declaration of Helsinki.

2.4. Statistical Considerations

As for continuous parameters, Student’s t test, Mann–Whitney U test or the Pearson correlation coefficient r were employed to assess between-group differences, as applicable. In categorical parameters, Fisher’s exact tests or the Pearson χ2 test was employed to assess between-group differences, as applicable. Factors with p < 0.1 for the correlation with the SF-36 scores across 10 items were subjected to multivariate regression analysis with multiple predictive variables by using the least squares method, to identify candidate parameters. Unless otherwise mentioned, data are indicated as number or average ± standard deviation (SD). All items of SF-36 were analyzed separately, and we considered variables of p < 0.05 as being statistically significant variables. The JMP 13.2 (SAS Institute Inc., Cary, NC, USA) was employed to carry out the statistical analysis.

3. Results

3.1. Patient Baseline Data

Baseline data in this study (n = 389, 198 men and 191 women, average age = 62.0 years) are indicated in Table 1. LC was found in 148 patients (38.0%). The average ± SD HGS and SMI in male patients were 33.6 ± 8.7 kg and 7.5 ± 1.1 kg/m2, respectively, and those in female patients were 20.9 ± 5.2 kg and 6.0 ± 0.7 kg/m2, respectively. Sarcopenia, as defined by the JSH criteria, was observed in 27 male patients (13.6%) and 34 female patients (17.8%) [18]. In LC patients, sarcopenia was identified in 39 patients (26.4%), while in non-LC patients, it was identified in 22 patients (9.1%).

Table 1.

Baseline characteristics.

Variables All Cases (n = 389) Decreased HGS (n = 93) Non-Decreased HGS (n = 296) p Value Decreased SMM (n = 159) Non-decreased SMM (n = 230) p Value
Age (years) 62.0 ± 12.8 69.7 ± 10.6 59.5 ± 12.5 <0.0001 66.7 ± 12.2 58.7 ± 12.2 <0.0001
Gender, male/female 198/191 36/57 162/134 0.0087 93/66 105/125 0.0135
Etiology, HBV/HCV/HBV, and HCV/NBNC 61/234/8/86 10/60/2/21 51/174/6/65 0.5130 21/101/5/32 40/133/3/54 0.3102
Presence of LC, yes/no 148/241 61/32 87/209 <0.0001 65/94 83/147 0.3416
Body mass index (kg/m2) 23.2 ± 3.8 22.7 ± 3.3 23.3 ± 4.0 0.1554 20.9 ± 2.4 24.8 ± 3.8 <0.0001
Total bilirubin (mg/dL) 0.96 ± 0.58 0.96 ± 0.62 0.96 ± 0.57 0.9545 0.86 ± 0.39 1.02 ± 0.68 0.0718
Serum albumin (g/dL) 4.1 ± 0.5 3.9 ± 0.57 4.2 ± 0.45 <0.0001 4.2 ± 0.48 4.1 ± 0.52 0.2688
Prothrombin time (%) 86.7 ± 16.6 84.1 ± 17.1 87.5 ± 16.3 0.0790 87.5 ± 16.9 86.1 ± 16.3 0.4112
Platelet count (×104/mm3) 16.8 ± 6.9 15.1 ± 6.5 17.3 ± 6.9 0.0081 16.7 ± 6.2 16.8 ± 7.3 0.7315
White blood cell (/mm3) 5165 ± 1614 5193 ± 1659 5156 ± 1602 0.8455 5240 ± 1466 5113 ± 1710 0.3114
Lymphocyte count (/mm3) 3112 ± 958 1395 ± 598 1627 ± 613 0.0015 1513 ± 542 1613 ± 661 0.2045
Total cholesterol (mg/dL) 181.3 ± 41.3 170.5 ± 47.2 184.7 ± 38.8 0.0038 182.0 ± 43.9 180.8 ± 39.5 0.7775
CONUT score 1.9 ± 1.9 2.7 ± 2.5 1.6 ± 1.6 0.0003 1.9 ± 1.7 1.9 ± 2.0 0.8450
AST (IU/L) 37.7 ± 27.3 40.3 ± 29.2 36.8 ± 26.6 0.2886 36.9 ± 26.1 38.2 ± 28.1 0.6286
ALT (IU/L) 37.3 ± 37.3 35.0 ± 38.4 38.1 ± 37.0 0.4966 35.4 ± 36.3 38.7 ± 38.0 0.3828
FIB-4 index 3.3 ± 3.3 4.0 ± 2.8 3.1 ± 3.4 0.0142 3.2 ± 2.2 3.4 ± 3.9 0.0215
Serum creatinine (mg/dL) 0.73 ± 0.54 0.76 ± 0.53 0.72 ± 0.55 0.4769 0.81 ± 0.81 0.67 ± 0.18 0.0095
HbA1c (NGSP) 5.9 ± 0.88 5.9 ± 0.80 5.8 ± 0.90 0.7085 5.9 ± 0.84 5.8 ± 0.90 0.7085
Serum sodium (mmol/L) 140.1 ± 2.3 139.9 ± 2.5 140.2 ± 2.3 0.2330 140.3 ± 2.4 140.0 ± 2.3 0.3413
HGS (kg), male 33.6 ± 8.7 22.0 ± 3.9 36.3 ± 6.4 <0.0001 29.4 ± 6.9 37.4 ± 7.5 <0.0001
HGS (kg), female 20.9 ± 5.2 14.8 ± 3.1 23.3 ± 3.6 <0.0001 18.2 ± 4.1 22.4 ± 5.1 <0.0001
SMI (kg/m2), male 7.5 ± 1.1 7.0 ± 0.97 7.6 ± 1.09 0.0039 6.8 ± 0.43 8.1 ± 1.13 <0.0001
SMI (kg/m2), female 6.0 ± 0.7 5.6 ± 0.74 6.1 ± 0.68 <0.0001 5.2 ± 0.39 6.4 ± 0.50 <0.0001

Data are expressed as average ± standard deviation. HBV; hepatitis B virus, HCV; hepatitis C virus, NBNC; non-B and non-C, LC; liver cirrhosis, CONUT score; controlling nutritional score, AST; aspartate aminotransferase, ALT; alanine aminotransferase, NGSP; National Glycohemoglobin Standardization Program, HGS; hand grip strength, SMM; skeletal muscle mass, SMI; skeletal muscle mass index.

Between-group differences (the d-HGS group (n = 93) vs. the non-decreased HGS (nd-HGS) group (n = 296)) were noted with statistical significance in age, gender, presence of LC, serum albumin, platelet count, lymphocyte count, total cholesterol, CONUT score, FIB-4 index, and SMI (both male and female). While in the d-SMM group (n = 159) vs. the non-decreased SMI (nd-SMM) group (n = 230), between-group differences in age, gender, body mass index (BMI), FIB-4 index, serum creatinine, and HGS (both male and female) reached significance. The corresponding average ± SD values and p values are listed in Table 1.

Between-group differences (LC patients (n = 148) vs. non-LC patients (n = 151)) were noted with statistical significance in the items of PF, RP, GH, VT, SF, RE, and PCS, suggesting that LC patients had poorer H-QOL compared with non-LC patients. Corresponding average ± SD values, 95% confidence intervals (CIs) and P values were summarized in Table 2.

Table 2.

Comparison of the SF-36 scores across 10 items in patients with LC and non-LC.

ALL Cases LC Patients (n = 148) Non-LC Patients (n = 241) p Value
PF 79.9 ± 20.2 [76.6, 83.2] 87.5 ± 15.8 [85.5, 89.5] <0.0001
RP 77.0 ± 30.7 [72.0, 82.0] 87.2 ± 21.4 [84.5, 90.0] 0.0005
BP 71.6 ± 26.1 [67.3, 75.9] 76.3 ± 23.9 [73.3, 79.3] 0.0709
GH 51.6 ± 19.7 [48.4, 54.8] 58.4 ± 19.1 [55.9, 60.9] 0.0011
VT 59.3 ± 22.6 [55.6, 63.0] 67.6 ± 20.5 [65.0, 70.2] 0.0002
SF 82.9 ± 25.1 [78.8, 87.0] 89.4 ± 19.4 [86.9, 91.9] 0.0004
RE 78.6 ± 28.3 [74.0, 83.3] 88.1 ± 21.4 [85.4, 90.8] <0.0001
MH 73.0 ± 20.6 [69.6, 76.4] 74.9 ± 20.7 [72.2, 77.5] 0.3845
PCS 42.3 ± 16.2 [39.6, 45.1] 48.7 ± 11.9 [47.1, 50.2] <0.0001
MCS 49.9 ± 10.1 [48.2, 51.6] 51.8 ± 10.4 [50.4, 53.1] 0.0891

Data are expressed as average ± standard deviation and 95% confidence interval. LC; liver cirrhosis, PF; physical functioning, RP; role physical, BP; bodily pain, GH; general health perception, VT; vitality, SF; social functioning, RE; role emotion, MH; mental health, PCS; physical component summary score, MCS; mental component summary score.

3.2. Impact of HGS and SMM on the SF-36 Scores for all Cases

The average ± SD SF-36 scores (95% CIs) in the d-HGS and nd-HGS groups (n = 93 and 296), and the d-SMM and nd-SMM groups (n = 159 and 230) for all cases are presented in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p < 0.0001), RP (p < 0.0001), BP (p = 0.0043), VT (p = 0.0011), SF (p < 0.0001), RE (p < 0.0001), and PCS (p < 0.0001) reached significance, while SF-36 scores in the d-SMI group were significantly higher than those in the nd-SMI group in the items of PF (p = 0.0032), SF (p = 0.0031) and RE (p = 0.0030). (Figure 1a,b).

Table 3.

Comparison of the SF-36 scores across 10 items.

ALL Cases Decreased HGS (n = 93) Non-Decreased HGS (n = 296) p Value
PF 72.8 ± 22.6 [68.1, 77.5] 88.3 ± 14.3 [86.7, 90.0] <0.0001
RP 70.6 ± 33.1 [63.7, 77.4] 87.3 ± 21.7 [84.8, 89.8] <0.0001
BP 68.1 ± 24.0 [63.2, 73.1] 76.5 ± 24.8 [73.7, 79.4] 0.0043
GH 54.8 ± 22.7 [50.1, 59.5] 56.1 ± 18.5 [53.9, 58.2] 0.6190
VT 57.7 ± 25.1 [52.5, 62.9] 66.6 ± 20.0 [64.3, 68.9] 0.0011
SF 79.5 ± 25.4 [74.2, 84.8] 89.3 ± 20.2 [86.9, 91.6] <0.0001
RE 72.4 ± 30.3 [66.1, 78.8] 88.3 ± 21.2 [85.9, 90.7] <0.0001
MH 72.3 ± 24.1 [67.3, 77.3] 74.7 ± 19.4 [72.5, 77.0] 0.7439
PCS 37.3 ± 16.7 [33.8, 40.8] 49.2 ± 11.7 [47.8, 50.6] <0.0001
MCS 50.5 ± 11.0 [48.2, 52.9] 51.2 ± 10.1 [50.5, 52.4] 0.5941
ALL Cases Decreased SMM (n = 159) Non-Decreased SMM (n = 230) p Value
PF 81.3 ± 18.1 [78.5, 84.2] 86.8 ± 17.5 [84.6, 89.1] 0.0032
RP 80.4 ± 27.2 [76.2, 84.7] 85.3 ± 24.7 [82.1, 88.6] 0.0660
BP 74.7 ± 25.1 [70.8, 78.7] 74.4 ± 24.6 [71.2, 77.6] 0.8891
GH 55.2 ± 20.4 [52.0, 58.5] 56.1 ± 19.1 [53.6, 58.7] 0.6656
VT 62.6 ± 23.6 [58.9, 66.3] 65.8 ± 20.2 [63.2, 68.4] 0.3364
SF 84.9 ± 24.7 [80.9, 88.8] 88.3 ± 19.7 [85.7, 91.0] 0.0031
RE 82.0 ± 26.6 [77.8, 86.1] 86.4 ± 23.0 [83.3, 89.4] 0.0030
MH 72.7 ± 22.4 [69.2, 76.2] 75.2 ± 19.3 [72.7, 77.7] 0.4683
PCS 45.3 ± 14.2 [43.0, 47.6] 47.0 ± 13.9 [45.1, 48.8] 0.2610
MCS 51.3 ± 10.5 [49.6, 53.0] 50.8 ± 10.1 [49.5, 52.2] 0.6601
LC Decreased HGS (n = 61) Non-Decreased HGS (n = 87) p Value
PF 71.1 ± 23.1 [65.2, 77.1] 86.2 ± 15.0 [82.9, 89.4] 0.0002
RP 68.0 ± 34.0 [59.3, 76.7] 83.4 ± 26.5 [77.7, 89.1] 0.0006
BP 65.3 ± 22.8 [59.5, 71.2] 76.1 ± 27.5 [70.2, 82.0] 0.0002
GH 51.0 ± 19.9 [46.0, 56.1] 52.0 ± 19.7 [47.7, 56.3] 0.7691
VT 53.8 ± 23.7 [47.7, 59.9] 63.2 ± 21.1 [58.7, 67.7] 0.0132
SF 76.7 ± 26.8 [69.8, 83.6] 87.4 ± 22.9 [82.4, 92.3] 0.0112
RE 67.2 ± 30.9 [59.3, 75.2] 86.7 ± 23.3 [81.7, 91.7] <0.0001
MH 71.1 ± 22.8 [65.2, 77.0] 74.3 ± 18.9 [70.3, 78.4] 0.3514
PCS 34.9 ± 16.5 [30.7, 39.2] 47.9 ± 13.7 [44.8, 50.9] <0.0001
MCS 49.3 ± 9.7 [46.8, 51.8] 50.3 ± 10.5 [48.0, 52.7] 0.5382
LC Decreased SMM (n = 66) Non-Decreased SMM (n = 82) p Value
PF 75.7 ± 20.7 [70.5, 80.8] 83.2 ± 19.2 [79.0, 87.4] 0.0252
RP 72.1 ± 31.6 [64.3, 80.0] 80.9 ± 29.6 [74.4, 87.4] 0.0867
BP 72.3 ± 26.1 [65.8, 78.8] 71.1 ± 26.3 [65.3, 76.8] 0.7832
GH 51.0 ± 20.0 [46.1, 56.0] 52.1 ± 19.6 [47.7, 56.4] 0.7589
VT 56.3 ± 24.3 [50.2, 62.4] 61.7 ± 21.0 [57.1, 66.3] 0.1519
SF 81.1 ± 28.4 [74.1, 88.3] 84.3 ± 22.1 [79.4, 89.2] 0.4615
RE 73.1 ± 31.9 [65.2, 81.1] 83.0 ± 24.4 [77.6, 88.4] 0.0131
MH 71.1 ± 23.7 [65.2, 77.0] 74.5 ± 17.8 [70.6, 78.4] 0.6602
PCS 41.5 ± 17.2 [37.2, 45.8] 43.0 ± 15.5 [39.5, 46.6] 0.5729
MCS 50.4 ± 10.4 [47.8, 53.1] 49.4 ± 9.9 [47.2, 51.7] 0.5615
Non-LC Decreased HGS (n = 32) Non-Decreased HGS (n = 209) p Value
PF 76.1 ± 21.6 [68.1, 84.0] 89.2 ± 14.0 [87.3, 91.1] <0.0001
RP 75.7 ± 30.9 [64.4, 87.1] 88.9 ± 19.2 [86.3, 91.6] <0.0001
BP 73.5 ± 25.6 [64.3, 82.7] 76.7 ± 23.6 [73.5, 79.9] 0.4782
GH 62.0 ± 26.2 [52.5, 71.5] 57.8 ± 17.7 [55.3, 60.3] 0.0876
VT 65.0 ± 26.5 [55.5, 74.6] 68.0 ± 19.4 [65.4, 70.7] 0.4422
SF 84.9 ± 22.1 [76.8, 93.0] 90.1 ± 18.9 [87.5, 92.7] 0.1629
RE 82.5 ± 27.0 [72.6, 92.4] 89.0 ± 20.3 [86.2, 91.7] 0.0002
MH 74.6 ± 26.6 [65.0, 84.2] 74.9 ± 19.7 [72.2, 77.6] 0.4130
PCS 41.9 ± 16.4 [35.8, 48.0] 49.7 ± 10.6 [48.2, 51.2] 0.0018
MCS 53.1 ± 13.1 [48.2, 58.0] 51.6 ± 9.9 [40.2, 52.9] 0.3525
Non-LC Decreased SMM (n = 94) Non-Decreased SMM (n = 147) p Value
PF 85.3 ± 14.9 [82.2, 88.3] 88.9 ± 16.2 [86.3, 91.5] 0.0830
RP 86.2 ± 21.9 [81.7, 90.7] 87.9 ± 21.2 [84.4, 91.3] 0.5689
BP 76.6 ± 24.4 [71.4, 81.5] 76.2 ± 23.6 [72.4, 80.1] 0.9476
GH 58.3 ± 20.2 [54.0, 62.5] 58.4 ± 18.5 [55.4, 61.5] 0.9482
VT 66.9 ± 22.2 [62.4, 71.5] 68.1 ± 19.4 [64.9, 71.2] 0.6748
SF 87.7 ± 21.5 [83.0, 91.9] 90.7 ± 17.8 [87.7, 93.6] 0.2185
RE 87.9 ± 20.5 [83.8, 92.1] 88.2 ± 22.0 [84.6, 91.8] 0.9205
MH 73.8 ± 21.5 [69.3, 78.2] 75.6 ± 20.2 [72.3, 78.9] 0.5102
PCS 48.0 ± 11.1 [45.7, 50.3] 49.1 ± 12.4 [47.1, 51.2] 0.4689
MCS 52.0 ± 10.6 [49.7, 54.2] 51.6 ± 10.2 [49.9, 53.3] 0.8203
Male Decreased HGS (n = 36) Non-Decreased HGS (n = 162) p Value
PF 72.9 ± 23.7 [64.9, 80.9] 88.9 ± 13.9 [86.7, 91.1] <0.0001
RP 69.8 ± 34.9 [58.0, 81.6] 88.6 ± 20.1 [85.4, 91.7] <0.0001
BP 72.2 ± 26.0 [63.4, 81.0] 78.9 ± 23.6 [75.2, 82.5] 0.1328
GH 55.1 ± 23.1 [47.3, 62.9] 54.7 ± 18.3 [51.8, 57.6] 0.9145
VT 60.2 ± 26.3 [51.1, 69.2] 65.8 ± 20.5 [62.7, 69.0] 0.1614
SF 81.2 ± 27.2 [71.8, 90.5] 88.9 ± 20.3 [85.7, 92.1] <0.0001
RE 71.5 ± 33.2 [60.1, 82.9] 88.9 ± 20.8 [85.6, 92.1] <0.0001
MH 74.8 ± 24.0 [66.6, 83.1] 72.9 ± 20.0 [69.7, 76.0] 0.6112
PCS 37.0 ± 18.7 [30.6, 43.4] 50.4 ± 11.6 [48.5, 52.3] <0.0001
MCS 52.7 ± 11.5 [48.8, 56.7] 50.1 ± 10.3 [48.4, 51.7] 0.1817
Male Decreased SMM (n = 92) Non-Decreased SMM (n = 106) p Value
PF 83.4 ± 16.5 [80.0. 86.8] 88.3 ± 17.5 [84.9, 91.7] 0.0451
RP 81.6 ± 26.8 [76.1, 87.1] 88.3 ± 21.8 [84.1, 92.6] 0.0035
BP 77.1 ± 24.8 [72.0, 82.2] 78.2 ± 23.6 [73.6, 82.7] 0.7508
GH 53.9 ± 20.9 [49.6, 58.3] 55.5 ± 17.8 [52.0, 59.0] 0.5712
VT 63.6 ± 24.5 [58.6, 68.7] 65.9 ± 18.9 [62.2, 69.5] 0.9880
SF 85.3 ± 25.0 [80.1, 90.5] 89.5 ± 18.6 [85.8, 93.1] 0.0507
RE 82.6 ± 27.1 [77.0, 88.2] 88.5 ± 21.3 [84.4, 92.7] 0.0904
MH 73.2 ± 22.5 [68.6, 77.9] 73.2 ± 19.2 [69.5, 76.9] 0.9942
PCS 46.3 ± 14.6 [43.3, 49.4] 49.4 ± 13.7 [46.6, 52.1] 0.1419
MCS 51.1 ± 11.2 [48.7, 53.4] 50.1 ± 10.1 [48.1, 52.1] 0.5428
Female Decreased HGS (n = 57) Non-Decreased HGS (n = 134) p Value
PF 72.7 ± 22.1 [66.8, 78.7] 87.6 ± 14.9 [85.0, 90.1] <0.0001
RP 71.1 ± 32.2 [62.5, 79.7] 85.8 ± 23.4 [81.8, 89.8] <0.0001
BP 65.6 ± 22.5 [59.6, 71.6] 73.6 ± 25.9 [69.2, 78.1] 0.0432
GH 54.6 ± 22.7 [48.6, 60.6] 57.8 ± 18.6 [54.5, 61.0] 0.3266
VT 56.2 ± 24.5 [49.7, 62.7] 67.5 ± 19.4 [64.2, 70.9] 0.0006
SF 78.4 ± 24.5 [71.9, 85.0] 89.7 ± 20.1 [86.2, 93.3] 0.0012
RE 73.0 ± 8.7 [65.3, 80.7] 87.6 ± 21.7 [83.9, 91.3] <0.0001
MH 70.8 ± 24.3 [64.3, 77.2] 77.1 ± 18.5 [73.9, 80.3] 0.1394
PCS 37.4 ± 15.5 [33.2, 41.6] 47.7 ± 11.6 [45.7, 49.8] <0.0001
MCS 49.2 ± 10.5 [46.3, 52.0] 52.6 ± 9.6 [50.9, 54.3] 0.0326
Female Decreased SMM (n = 66) Non-Decreased SMM (n = 125) p Value
PF 78.5 ± 19.9 [73.6, 83.5] 85.6 ± 17.5 [82.5, 88.7] 0.0124
RP 78.8 ± 27.8 [71.9, 85.7] 82.8 ± 26.7 [78.1, 87.6] 0.3273
BP 71.3 ± 25.3 [65.0, 77.6] 71.1 ± 25.2 [66.7, 75.6] 0.9672
GH 57.1 ± 19.7 [52.2, 62.0] 56.6 ± 20.2 [53.0, 60.3] 0.8853
VT 61.1 ± 22.3 [55.6, 66.6] 65.7 ± 21.2 [61.9, 69.5] 0.1652
SF 84.2 ± 24.5 [78.2, 90.3] 87.4 ± 20.6 [83.7, 91.2] 0.3527
RE 81.0 ± 26.2 [74.6, 87.5] 84.5 ± 24.1 [80.3, 88.8] 0.3546
MH 71.9 ± 22.4 [66.4, 77.5] 76.9 ± 19.4 [73.4, 80.3] 0.1161
PCS 43.9 ± 13.7 [40.4, 47.3] 45.0 ± 13.8 [42.5, 47.5] 0.5979
MCS 51.7 ± 9.7 [49.3, 54.1] 51.5 ± 10.2 [49.6, 53.3] 0.8719
≥65 years Decreased HGS (n = 74) Non-Decreased HGS (n = 121) p Value
PF 72.8 ± 23.5 [67.3, 78.3] 84.9 ± 14.0 [82.3, 87.4] 0.0001
RP 68.8 ± 34.6 [60.8, 76.9] 86.3 ± 20.6 [82.6, 90.1] <0.0001
BP 68.8 ± 24.3 [63.2, 74.4] 78.0 ± 24.1 [73.6, 82.4] 0.0111
GH 57.6 ± 23.3 [52.2, 63.0] 56.8 ± 18.9 [53.3, 60.3] 0.7950
VT 57.9 ± 25.7 [52.0. 63.9] 68.9 ± 19.8 [65.3, 72.5] 0.0021
SF 78.3 ± 25.1 [72.5, 84.1] 91.1 ± 18.3 [87.7, 94.4] <0.0001
RE 71.5 ± 30.6 [64.4, 78.7] 88.0 ± 20.5 [84.2, 91.7] <0.0001
MH 73.0 ± 25.1 [67.2, 78.8] 77.4 ± 17.9 [74.1, 80.6] 0.5509
PCS 36.5 ± 17.6 [32.4, 40.6] 47.2 ± 10.1 [45.3, 49.1] <0.0001
MCS 51.5 ± 11.2 [48.9, 54.1] 53.5 ± 9.2 [51.8, 55.2] 0.1822
≥65 years Decreased SMM (n = 110) Non-Decreased SMM (n = 85) p Value
PF 78.5 ± 18.6 [75.0, 82.1] 82.6 ± 19.4 [78.4, 86.8] 0.1435
RP 78.3 ± 28.6 [72.8, 83.7] 81.6 ± 27.4 [75.6, 87.5] 0.4226
BP 73.9 ± 26.2 [68.9, 78.9] 75.2 ± 22.4 [70.3, 80.0] 0.7338
GH 56.6 ± 21.9 [52.4, 60.8] 57.8 ± 19.0 [53.6, 62.0] 0.6926
VT 62.8 ± 24.4 [58.2, 67.4] 67.2 ± 20.6 [62.8, 71.7] 0.1809
SF 85.5 ± 23.8 [80.9, 90.0] 86.9 ± 19.5 [82.6, 91.2] 0.6548
RE 80.1 ± 27.3 [74.9, 85.2] 83.9 ± 24.2 [78.6, 89.3] 0.3090
MH 74.0 ± 22.3 [69.8, 78.2] 77.9 ± 19.1 [73.8, 82.1] 0.1972
PCS 43.3 ± 14.1 [40.6, 45.9] 42.7 ± 15.2 [39.3, 46.1] 0.7951
MCS 52.8 ± 10.1 [50.9, 54.7] 52.6 ± 10.1 [50.4, 54.9] 0.9288
<65 years Decreased HGS (n = 19) Non-Decreased HGS (n = 175) p Value
PF 72.8 ± 19.6 [63.3, 82.2] 90.7 ± 14.1 [88.6, 92.8] <0.0001
RP 77.3 ± 25.9 [64.8, 89.8] 88.0 ± 22.4 [84.6, 91.3] 0.0530
BP 65.5 ± 23.1 [54.4, 76.7] 75.5 ± 25.2 [71.8, 79.3] 0.0990
GH 44.0 ± 16.9 [35.8, 52.1] 55.6 ± 18.3 [52.8, 58.4] 0.0088
VT 56.8 ± 23.2 [45.3, 68.3] 65.0 ± 20.0 [62.0, 68.0] 0.1042
SF 84.6 ± 27.1 [70.7, 98.6] 88.1 ± 21.3 [84.9, 91.3] 0.5338
RE 76.2 ± 29.8 [61.4, 91.0] 88.5 ± 21.7 [85.3, 91.8] 0.0281
MH 69.4 ± 20.2 [59.3, 79.4] 73.0 ± 20.3 [70.0, 76.0] 0.4708
PCS 40.5 ± 11.8 [34.4, 46.6] 50.5 ± 12.5 [48.6, 52.4] 0.0018
MCS 46.5 ± 9.4 [41.7, 51.3] 49.6 ± 10.3 [48.1, 51.2] 0.2286
<65 years Decreased SMM (n = 49) Non-Decreased SMM (n = 145) p Value
PF 87.7 ± 15.1 [83.4, 92.1] 89.3 ± 15.8 [86.7, 91.9] 0.5386
RP 85.2 ± 23.3 [78.6, 91.9] 87.5 ± 22.8 [83.8, 91.3] 0.5501
BP 76.5 ± 22.8 [69.9, 83.0] 73.9 ± 25.9 [69.7, 78.2] 0.5389
GH 52.0 ± 16.1 [47.3, 56.8] 55.2 ± 19.1 [52.0, 58.4] 0.3182
VT 62.2 ± 21.9 [55.8, 68.5] 65.0 ± 19.9 [61.7, 68.2] 0.4133
SF 83.4 ± 26.9 [75.5, 91.4] 89.2 ± 19.8 [85.9, 92.5] 0.0286
RE 86.3 ± 24.8 [79.1, 93.5] 87.7 ± 22.2 [84.1, 91.4] 0.7097
MH 69.7 ± 22.5 [63.2, 76.3] 73.6 ± 19.4 [70.4, 76.8] 0.2510
PCS 50.2 ± 13.6 [46.1, 54.3] 49.4 ± 12.5 [47.3, 51.5] 0.7120
MCS 47.9 ± 10.9 [44.6, 51.1] 49.8 ± 10.0 [48.2, 51.5] 0.2593

Data are expressed as average ± standard deviation and 95% confidence interval. HGS; hand grip strength, SMM; skeletal muscle mass, LC; liver cirrhosis, PF; physical functioning, RP; role physical, BP; bodily pain, GH; general health perception, VT; vitality, SF; social functioning, RE; role emotion, MH; mental health, PCS; physical component summary score, MCS; mental component summary score.

Figure 1.

Figure 1

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) for all cases (n = 389). The average scores in each item of the SF-36 were plotted.

3.3. Subgroup Analysis 1: Impact of HGS and SMM on the SF-36 Scores for LC Patients

The average ± SD SF-36 scores [95% CIs] in the d-HGS and nd-HGS groups (n = 61 and 87), and the d-SMM and nd-SMM groups (n = 66 and 82) for LC patients are shown in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p = 0.0002), RP (p = 0.0006), BP (p = 0.0002), VT (p = 0.0132), SF (p = 0.0112), RE (p < 0.0001), and PCS (p < 0.0001) reached significance, while in the d-SMM group vs. the nd-SMI group, the differences were noted with significance in the items of PF (p = 0.0252) and RE (p = 0.0131) (Figure 2a,b).

Figure 2.

Figure 2

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in LC patients (n = 148). The average scores in each item of the SF-36 were plotted.

3.4. Subgroup Analysis 2: Impact of HGS and SMM on the SF-36 Scores for Non-LC Patients

The average ± SD SF-36 scores (95% CIs) in the d-HGS and nd-HGS groups (n = 32 and 209) and the d-SMM and nd-SMM groups (n = 94 and 147) for non-LC patients are demonstrated in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p = 0.0002), RP (p = 0.0006), RE (p = 0.0002), and PCS (p = 0.0018) reached significance, while in the d-SMM group vs. the nd-SMM group, no significant difference was noted in all items (Figure 3a,b).

Figure 3.

Figure 3

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in non-LC patients (n = 241). The average scores in each item of the SF-36 were plotted.

3.5. Subgroup Analysis 3: Impact of HGS and SMM on the SF-36 Scores for Male Patients

The average ± SD SF-36 scores (95% CIs) in the d-HGS and nd-HGS groups (n = 36 and 162) and the d-SMM and nd-SMM groups (n = 92 and 106) for male patients are indicated in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p < 0.0001), RP (p < 0.0001), SF (p < 0.0001), RE (p < 0.0001) and PCS (p < 0.0001) reached significance, while the SF-36 scores in the d-SMM group were significantly higher than those in the nd-SMM group in the items of PF (p = 0.0451) and RP (p = 0.0035) (Figure 4a,b).

Figure 4.

Figure 4

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in male patients (n = 198). The average scores in each item of the SF-36 were plotted.

3.6. Subgroup Analysis 4: Impact of HGS and SMM on the SF-36 Scores for Female Patients

The average ± SD SF-36 scores [95% CIs] in the d-HGS and nd-HGS groups (n = 57 and 134) and the d-SMM and nd-SMM groups (n = 66 and 125) for female patients are indicated in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p < 0.0001), RP (p < 0.0001), BP (p = 0.0432), VT (p = 0.0006), SF (p = 0.0012), RE (p < 0.0001), PCS (p < 0.0001) and MCS (p = 0.0326) reached significance, while in the d-SMM group vs. the nd-SMI group, the difference was observed with significance only in the item of PF (p = 0.0124). (Figure 5a,b).

Figure 5.

Figure 5

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in female patients (n = 191). The average scores in each item of the SF-36 were plotted.

3.7. Subgroup Analysis 5: Impact of HGS and SMM on the SF-36 Scores for Patients Aged ≥65 Years

The average ± SD SF-36 scores (95% CIs) in the d-HGS and nd-HGS groups (n = 74 and 121) and the d-SMM and nd-SMM groups (n = 110 and 85) for patients aged ≥65 years are indicated in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p = 0.0001), RP (p < 0.0001), BP (p = 0.0111), VT (p = 0.0021), SF (p < 0.0001), RE (p < 0.0001), and PCS (p < 0.0001) reached significance, while in the d-SMM group vs. the nd-SMM group, no significant differences were observed in all items (Figure 6a,b).

Figure 6.

Figure 6

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in patients aged >65 years (n = 195). The average scores in each item of the SF-36 were plotted.

3.8. Subgroup Analysis 6: Impact of HGS and SMM on the SF-36 Scores for Patients Aged <65 Years

The average ± SD SF-36 scores (95% CIs) in the d-HGS and nd-HGS groups (n = 19 and 175) and the d-SMM and nd-SMM groups (n = 49 and 145) in patients aged <65 years are indicated in Table 3. Between-group differences (the d-HGS group vs. the nd-HGS group) in the items of PF (p < 0.0001), GH (p = 0.0088), RE (p = 0.0281), and PCS (p = 0.0081) reached significance, while in the d-SMM group vs. the nd-SMM group, between-group difference was significant only in the item of SF (p = 0.0286) (Figure 7a,b).

Figure 7.

Figure 7

The SF-36 scores across 10 items in the decreased and non-decreased HGS groups (a), and the decreased and non-decreased SMM groups (b) in patients aged <65 years (n = 194). The average scores in each item of the SF-36 were plotted.

3.9. Relationship between the SF-36 Scores and Baseline Parameters in Male Patients and Female Patients

Correlation coefficients and p values between the SF-36 scores across 10 items, and baseline parameters in male patients and female patients are summarized in Table 4.

Table 4.

Relationship between baseline data and the SF-36 scores in each item in male and female patients.

Male PF RP BP GH VT
r p Value r p Value r p Value r p Value r p Value
Age −0.21 0.0036 −0.12 0.0939 −0.12 0.0869 0.11 0.1298 0.069 0.3346
BMI −0.057 0.4246 −0.051 0.4740 −0.047 0.5091 0.039 0.5925 −0.044 0.5394
HGS 0.32 <0.0001 0.25 0.0007 0.048 0.5242 −0.016 0.8924 0.0058 0.9383
SMI −0.0066 0.9268 −0.0028 0.9685 −0.081 0.2577 −0.00035 0.9961 −0.062 0.3920
Albumin 0.42 <0.0001 0.38 <0.0001 0.21 0.0025 0.18 0.0143 0.25 0.0005
Bilirubin 0.011 0.8784 −0.021 0.7731 −0.041 0.5686 −0.061 0.4026 −0.0278 0.7018
PT 0.26 0.0002 0.16 0.0245 0.063 0.3773 0.17 0.0209 0.19 0.0086
Platelet 0.11 0.1250 0.042 0.5583 −0.031 0.6653 0.11 0.1449 0.020 0.7802
CONUT −0.4 <0.0001 −0.30 <0.0001 −0.12 0.0924 −0.17 0.0164 −0.17 0.0181
AST −0.01 0.1626 −0.27 0.0013 −0.15 0.0412 −0.21 0.0030 −0.16 0.0220
ALT −0.027 0.7035 −0.18 0.0104 −0.11 0.1393 −0.17 0.0189 −0.13 0.0707
Male SF RE MH PCS MCS
r p Value r p Value r p Value r p Value r p Value
Age −0.019 0.7916 −0.064 0.3732 0.14 0.0509 −0.24 0.0011 0.22 0.0030
BMI −0.046 0.5294 0.055 0.4441 0.031 0.6637 −0.083 0.260 0.0099 0.8930
HGS 0.10 0.1827 0.16 0.0324 −0.10 0.1772 0.29 0.0001 −0.16 0.0353
SMI −0.043 0.5601 0.056 0.4391 0.046 0.5193 −0.050 0.4976 −0.02 0.7834
Albumin 0.27 0.0002 0.33 <0.0001 0.086 0.2273 0.46 <0.0001 0.046 0.5348
Bilirubin −0.064 0.3845 −0.0071 0.9215 0.067 0.3569 −0.02 0.7925 −0.035 0.6371
PT 0.16 0.0286 0.10 0.1503 0.020 0.7849 0.19 0.0088 0.069 0.3468
Platelet 0.10 0.1614 −0.040 0.5762 −0.1243 0.0818 0.051 0.4905 −0.023 0.7590
CONUT −0.19 0.0091 −0.21 0.0031 0.026 0.7197 0.36 <0.0001 0.011 0.8773
AST −0.070 0.3345 −0.19 0.0071 −0.13 0.0675 −0.16 0.0286 −0.12 0.1021
ALT −0.025 0.7311 −0.20 0.0050 −0.15 0.0331 0.10 0.1650 −0.11 0.1172
Female PF RP BP GH VT
r p Value r p Value r p Value r p Value r p Value
Age −0.25 0.0004 −0.15 0.0384 0.051 0.4835 0.077 0.2987 −0.035 0.6346
BMI −0.037 0.6128 −0.0065 0.9292 −0.025 0.7329 −0.0248 0.7383 0.0059 0.9357
HGS 0.35 <0.0001 0.18 0.0195 0.098 0.1953 0.054 0.4815 0.23 0.0022
SMI 0.20 0.0053 0.10 0.1677 −0.048 0.5136 −0.0055 0.9409 0.096 0.1877
Albumin 0.24 0.0011 0.27 0.0002 0.15 0.0407 0.16 0.0351 0.20 0.0058
Bilirubin −0.078 0.2909 −0.18 0.0133 −0.13 0.0711 −0.092 0.2216 −0.11 0.1427
PT 0.021 0.7759 0.12 0.0978 0.066 0.3663 0.088 0.2349 0.14 0.0552
Platelet 0.11 0.1247 0.13 0.080 0.069 0.3444 0.040 0.5908 0.083 0.2585
CONUT −0.2 0.0051 −0.27 0.0002 −0.16 0.0246 −0.19 0.0088 −0.15 0.0423
AST −0.11 0.1441 −0.12 0.1023 −0.10 0.1521 −0.094 0.2403 −0.17 0.0181
ALT −0.03 0.6782 −0.039 0.5944 −0.14 0.0507 −0.087 0.2403 −0.13 0.0662
Female SF RE MH PCS MCS
r p Value r p Value r p Value r p Value r p Value
Age 0.017 0.8212 −0.11 0.1373 −0.021 0.7774 −0.20 0.0066 0.097 0.1948
BMI −0.012 0.8759 −0.0045 0.9511 −0.0075 0.9186 −0.062 0.4035 −0.044 0.5541
HGS 0.18 0.0179 0.19 0.0112 0.17 0.0222 0.28 0.0003 0.15 0.0446
SMI 0.025 0.7319 0.11 0.1375 0.057 0.4395 0.087 0.2433 −0.060 0.4255
Albumin 0.20 0.0072 0.19 0.0098 0.12 0.0878 0.30 <0.0001 0.15 0.0481
Bilirubin −0.18 0.0148 −0.16 0.0304 −0.04 0.5927 −0.21 0.0043 −0.074 0.3295
PT 0.14 0.0503 0.13 0.0766 0.12 0.1036 0.12 0.1030 0.19 0.0119
Platelet 0.098 0.1837 0.12 0.1067 0.12 0.1103 0.16 0.0311 0.093 0.2115
CONUT −0.17 0.0253 −0.17 0.0206 0.081 0.2708 −0.31 <0.0001 −0.11 0.1407
AST −0.16 0.0336 −0.13 0.0719 −0.16 0.0245 −0.11 0.1386 −0.17 0.0206
ALT −0.084 0.2597 −0.051 0.4811 −0.98 0.1817 −0.025 0.7397 −0.15 0.0462

PF; physical functioning, RP; role physical, BP; bodily pain, GH; general health perception, VT; vitality, SF; social functioning, RE; role emotion, MH; mental health, PCS; physical component summary score, MCS; mental component summary score, BMI; body mass index, HGS; hand grip strength, SMI; skeletal muscle mass index, PT; prothrombin time, CONUT; controlling nutritional score, AST; aspartate aminotransferase, ALT; alanine aminotransferase.

In male patients, HGS significantly correlated with PF (r = 0.32, p < 0.0001), RP (r = 0.25, p = 0.0007), RE (r = 0.16, p = 0.0324), and PCS (r = 0.29, p < 0.0001), while SMI did not significantly correlate with any item. Serum albumin level significantly correlated with all items other than MH and HCS.

In female patients, HGS significantly correlated with PF (r = 0.35, p < 0.0001), RP (r = 0.18, p = 0.0195), VT (r = 0.23, p = 0.0022), SF (r = 0.18, p = 0.0179), RE (r = 0.19, p = 0.0112), MH (r = 0.17, p = 0.0222), PCS (r = 0.28, p = 0.0003), and MCS (r = 0.15, p = 0.0446), whereas SMI significantly correlated with PF only (r = 0.20, p = 0.0053). Serum albumin levels significantly correlated with all items other than MH.

3.10. Multivariate Analyses of Factors Linked to the SF-36 Scores in Male Patients and Female Patients

In male patients, multivariate analyses of factors for the SF-36 scores revealed that HGS was significantly linked to PF (p = 0.0031), RP (p = 0.0185) and PCS (p = 0.0421), while serum albumin was a significant factor for PF (p = 0.0048), RP (p = 0.0004), VT (p = 0.0327), SF (p = 0.0085), RE (p = 0.0002) and PCS (p < 0.0001) (Table 5).

Table 5.

Multivariate analyses of factors linked to the SF-36 scores in male and female patients.

Male Parameter (Significant Factor Only) Estimates Standard Error p Value
PF HGS 0.494 0.104 0.0031
Serum albumin 9.008 3.152 0.0048
CONUT score −1.656 0.796 0.0389
RP HGS 0.579 0.244 0.0185
Serum albumin 17.593 4.899 0.0004
BP NA NA NA NA
GH NA NA NA NA
VT Serum albumin 8.944 4.158 0.0327
SF Serum albumin 10.456 3.929 0.0085
RE Serum albumin 18.765 4.891 0.0002
ALT −0.245 0.0845 0.0042
MH NA NA NA NA
PCS HGS 0.288 0.141 0.0421
Serum albumin 11.016 2.692 <0.0001
MCS NA NA NA NA
Female Parameter (significant factor only) Estimates Standard error p Value
PF HGS 0.958 0.322 0.0034
RP NA NA NA NA
BP NA NA NA NA
GH NA NA NA NA
VT HGS 0.851 0.346 0.0150
SF NA NA NA NA
RE HGS 0.729 0.36 0.0422
MH AST −0.124 0.0609 0.0440
PCS HGS 0.521 0.22 0.0191
MCS NA NA NA NA

PF; physical functioning, RP; role physical, BP; bodily pain, GH; general health perception, VT; vitality, SF; social functioning, RE; role emotion, MH; mental health, PCS; physical component summary score, MCS; mental component summary score, HGS; hand grip strength, CONUT score; controlling nutritional score, NA; not applicable, ALT; alanine aminotransferase, AST; aspartate aminotransferase.

In female patients, multivariate analyses of factors for the SF-36 scores revealed that HGS was significantly linked to PF (p = 0.0034), VT (p = 0.0150), RE (p = 0.0422), and PCS (p = 0.0191), whereas serum albumin did not significantly correlate with any item (Table 5).

4. Discussion

The loss of SMM in CLDs is caused by the progressive withdrawal of anabolism, and an increase in catabolism [34]. The liver is an essential organ that is involved in protein, fat, and carbohydrate metabolism, and energy generation [35,36]. H-QOL in CLDs has been demonstrated to be significantly compromised, and the decrease in H-QOL in CLDs is frequently overlooked or unrecognized [37]. To our knowledge, this is the first study demonstrating the relevance between HGS and SMM and H-QOL in CLD patients. To elucidate these issues is clinically of importance, because sarcopenia in liver diseases has been gaining much attention these days, due to its high prognostic predictability, and its definition includes HGS and SMM [18,19,20,21,22,23,24,25,26,27,28]. We therefore conducted the current analysis.

In our results, mean values in the d-HGS and nd-HGS groups were largely different, with statistical significance in the items of PF and PCS for all cases and all subgroup analyses, while in comparison, between the d-SMM and nd-SMM groups, such tendencies were not observed. Additionally, our multivariate analyses revealed that HGS was an independent predictor associated with PF and PCS irrespective of gender; however, in terms of mentality-related domains such as MH or MCS, both HGS and SMI appeared not to have an impact on the SF-36 scores. These results demonstrated that not SMM, but HGS has a strong influence on the physiological domains in the SF-36, which may be linked to clinical outcomes in CLD patients [11]. Numerous previous studies have reported that SMM is an independent outcome predictor in CLD patients [18,19,21,23,25,26]. However, reviewing our current results, decreased SMM itself is not possibly a prognostic factor, but the presence of a large number of patients with diminished muscle strength in diminished SMM patients leads to poor prognosis. Our data showing that SMI was significantly correlated with HGS, both in males (r = 0.37, p < 0.0001) and females (r = 0.46, p < 0.0001), support this hypothesis. In this respect, the current results seem to shed some insights on the better understanding of muscle mass and muscle weakness in CLD patients.

Notably, as presented in Table 1, age affected both HGS and SMI, while the presence of LC, serum albumin, and the CONUT score affected only HGS, and BMI affected only SMM. As described above, SMM decreases by approximately 1% after the age of 50 years, owing to changes in muscle fiber type and size [17]. These morphological and functional changes of skeletal muscle due to aging appear to account for the impact of aging on HGS and SMM. On the other hand, our current results denoted that d-SMM does not occur by poor nutritional state alone, and d-HGS does not occur by lower BMI alone, although the mechanisms for these remains unclear. In our comparison of the SF-36 scores across 10 items in patients with and without LC, significant differences were noted in numerous items, which are in agreement with previous reports [19,21,38,39]. LC patients tend to have worse H-QOL and exercise training can be a pivotal recommendation for LC patients [38]. While there have been few reports regarding H-QOL in non-LC patients. In that sense, our data are worthy of report.

In our multivariate analyses, serum albumin was an independent factor in several items of the SF-36 in male patients, while in female patients, serum albumin was not significant in any item of the SF-36. The average ± SD serum albumin levels in male and female in this study were 4.1 ± 0.53 g/dL and 4.2 ± 0.47 g/dL (p = 0.4726). Gender differences of hormones, including estrogen and progesterone or physiological and psychological attributes of men and women, may be attributed to our current results, however, it is likely that the ability of protein synthesis is associated with H-QOL in male CLD patients [40,41]. In our previous investigation, we have reported that serum levels of myostatin, which is a negative regulator of muscle protein synthesis, significantly differed in male and female LC patients [23].

The proportions of sarcopenia in LC and non-LC patients were 26.4% and 9.1%, respectively, in this study. Sarcopenia includes primary and secondary sarcopenia [18]. LC patients may have secondary sarcopenia due to impaired protein synthesis, and non-LC patients may have aging-related primary sarcopenia [18]. Clinicians should fully consider the etiology for sarcopenia in each patient.

Several limitations related to the study warrant mention. Firstly, the study was a single-center observational study with a retrospective nature. Secondly, the study data was derived from a Japanese liver disease population data, and additional investigations on other races are required to further verify and extend the application to other races. Thirdly, HGS can vary depending on patients’ daily life activities. Fourthly, patients with massive ascites or hepatic encephalopathy, who are potentially involved in sarcopenia were excluded, due to the lack of reliability in the BIA or the self-reported questionnaire, creating bias. Finally, the interpretation of our results should be done cautiously, since the direction of the association between the SF-36 scores and HGS or SMM remains unclear, due to the cross-sectional nature of our data. Nevertheless, our study results denoted that patients with d-HGS scored lower in the SF-36 vs. those with nd-HGS, especially in the physical health domains. In conclusion, HGS appears to have a strong impact on H-QOL in patients with CLDs, and exercise may be beneficial for improving H-QOL. In CLD patients with d-HGS, clinicians should be aware of the presence of CLD patients with decreased H-QOL.

5. Conclusions

HGS appears to have a strong impact on H-QOL in patients with CLDs.

Acknowledgments

The authors gratefully thank all medical staff in our nutritional guidance room for their help with data collection. No funding was provided for this study, and none of the authors has any conflicts of interest to declare.

Abbreviation

H-QOL health-related quality of life
CLD chronic liver disease
SF-36 36-Item Short Form Health Survey
SMM skeletal muscle mass
JSH Japanese Society of Hepatology
HGS hand grip strength
d-HGS decreased HGS
nd-HGS non-decreased HGS
BIA bioimpedance analysis
BMI body mass index
SMI skeletal muscle mass index
d-SMM decreased SMM
nd-SMM non-decreased SMM
LC liver cirrhosis
CONUT score controlling nutritional score
PF physical functioning
RP role physical
BP bodily pain
GH general health perception
VT vitality
SF social functioning
RE role emotion
MH mental health
PCS physical component summary score
MCS mental component summary score
SD standard deviation
CI confidence interval

Author Contributions

Data curation, K.Y., Y.I., Y.S., K.K., N.I. (Naoto Ikeda), T.T., N.A., R.T., K.H., N.I. (Noriko Ishii), Y.Y., T.N. and H.I.; Supervision, S.N.; Writing—Original draft, H.N.; Writing—Review & editing, H.E.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

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